Experimental estimates of germline mutation rate in eukaryotes: a phylogenetic meta-analysis.

IF 3.4 1区 生物学 Q2 EVOLUTIONARY BIOLOGY Evolution Letters Pub Date : 2023-08-01 DOI:10.1093/evlett/qrad027
Yiguan Wang, Darren J Obbard
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引用次数: 5

Abstract

Mutation is the ultimate source of all genetic variation, and over the last 10 years the ready availability of whole-genome sequencing has permitted direct estimation of mutation rate for many non-model species across the tree of life. In this meta-analysis, we make a comprehensive search of the literature for mutation rate estimates in eukaryotes, identifying 140 mutation accumulation (MA) and parent-offspring (PO) sequencing studies covering 134 species. Based on these data, we revisit differences in the single-nucleotide mutation (SNM) rate between different phylogenetic lineages and update the known relationships between mutation rate and generation time, genome size, and nucleotide diversity-while accounting for phylogenetic nonindependence. We do not find a significant difference between MA and PO in estimated mutation rates, but we confirm that mammal and plant lineages have higher mutation rates than arthropods and that unicellular eukaryotes have the lowest mutation rates. We find that mutation rates are higher in species with longer generation times and larger genome sizes, even when accounting for phylogenetic relationships. Moreover, although nucleotide diversity is positively correlated with mutation rate, the gradient of the relationship is significantly less than one (on a logarithmic scale), consistent with higher mutation rates in populations with smaller effective size. For the 29 species for which data are available, we find that indel mutation rates are positively correlated with nucleotide mutation rates and that short deletions are generally more common than short insertions. Nevertheless, despite recent progress, no estimates of either SNM or indel mutation rates are available for the majority of deeply branching eukaryotic lineages-or even for most animal phyla. Even among charismatic megafauna, experimental mutation rate estimates remain unknown for amphibia and scarce for reptiles and fish.

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真核生物种系突变率的实验估计:系统发育荟萃分析。
突变是所有遗传变异的最终来源,在过去的10年里,全基因组测序的可用性已经允许直接估计生命树中许多非模式物种的突变率。在这项荟萃分析中,我们对真核生物的突变率估计进行了全面的文献检索,鉴定了140个突变积累(MA)和亲代(PO)测序研究,涵盖134个物种。基于这些数据,我们重新审视了不同系统发育谱系之间单核苷酸突变率的差异,并更新了突变率与世代时间、基因组大小和核苷酸多样性之间的已知关系,同时考虑了系统发育的非独立性。我们没有发现MA和PO在估计突变率上的显著差异,但我们证实哺乳动物和植物谱系的突变率高于节肢动物,而单细胞真核生物的突变率最低。我们发现,即使考虑到系统发育关系,在世代时间较长、基因组大小较大的物种中,突变率也较高。此外,尽管核苷酸多样性与突变率呈正相关,但这种关系的梯度显著小于1(在对数尺度上),这与有效大小越小的种群突变率越高是一致的。在29个有数据的物种中,我们发现indel突变率与核苷酸突变率正相关,短缺失通常比短插入更常见。然而,尽管最近取得了进展,但对于大多数深分支真核生物谱系,甚至大多数动物门,都没有SNM或indel突变率的估计。即使在有魅力的巨型动物中,两栖动物的实验突变率估计仍然未知,爬行动物和鱼类的实验突变率估计也很少。
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来源期刊
Evolution Letters
Evolution Letters EVOLUTIONARY BIOLOGY-
CiteScore
13.00
自引率
2.00%
发文量
35
审稿时长
10 weeks
期刊介绍: Evolution Letters publishes cutting-edge new research in all areas of Evolutionary Biology. Available exclusively online, and entirely open access, Evolution Letters consists of Letters - original pieces of research which form the bulk of papers - and Comments and Opinion - a forum for highlighting timely new research ideas for the evolutionary community.
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